RETRACTED: miR-122 Regulates Tumorigenesis in Hepatocellular Carcinoma by Targeting AKT3 (Retracted article. See vol. 12, art no e0184778, 2017)

被引:71
|
作者
Nassirpour, Rounak [1 ]
Mehta, Pramod P. [1 ]
Yin, Min-Jean [1 ]
机构
[1] Pfizer Worldwide Res & Dev, Oncol Res, San Diego, CA USA
来源
PLOS ONE | 2013年 / 8卷 / 11期
关键词
HEPATITIS-C VIRUS; MICRORNA; EXPRESSION; GENOMICS; KINASE;
D O I
10.1371/journal.pone.0079655
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MicroRNAs (miRNAs) have been implicated in the orchestration of diverse cellular processes including differentiation, proliferation, and apoptosis and are believed to play pivotal roles as oncogenes and tumor suppressors. miR-122, a liver specific miRNA, is significantly down-regulated in most hepatocellular carcinomas (HCCs) but its role in tumorigenesis remains poorly understood. Here we identify AKT3 as a novel and direct target of miR-122. Restoration of miR-122 expression in HCC cell lines decreases AKT3 levels, inhibits cell migration and proliferation, and induces apoptosis. These anti-tumor phenotypes can be rescued by reconstitution of AKT3 expression indicating the essential role of AKT3 in miR-122 mediated HCC transformation. In vivo, restoration of miR-122 completely inhibited xenograft growth of HCC tumor in mice. Our data strongly suggest that miR-122 is a tumor suppressor that targets AKT3 to regulate tumorigenesis in HCCs and a potential therapeutic candidate for liver cancer.
引用
收藏
页数:10
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